Journal
FOOD CONTROL
Volume 136, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.foodcont.2022.108842
Keywords
Ochratoxin A; Gold nanoparticle; Peptide; Dot-blot assay; Detection
Categories
Funding
- Inspire Programme, Depart-ment of Science and Technology [BT/PR10455/PFN/20/869/2013]
- Department of Biotechnology
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In this study, a rapid and user-friendly dot-blot assay for the detection of ochratoxin A was developed using peptide conjugated gold nanoparticles as a detection agent. The assay exhibited high binding affinity towards ochratoxin A and had a low limit of detection. The dot-blot assay showed comparable results with the conventional high performance liquid chromatography in the detection of ochratoxin A in wheat samples. This portable and easy-to-use assay has the potential for application at different stages of food production and distribution to ensure safe and healthy food.
Ochratoxin A is a secondary metabolite produced by fungi and a major mycotoxin contaminating cereal grains and cereal-based products. Although, ochratoxin A is hepatotoxic, nephrotoxic and carcinogenic, its detection is limited due to low awareness, time-consuming conventional methods and false positive results. In this study, a rapid, user-friendly dot-blot assay was developed using peptide conjugated gold nanoparticles (AuNPs) as a detection agent. The peptide binding to ochratoxin A was evaluated by the apparent dissociation constant (K-d app) measurement using indirect enzyme linked immunoabsorbent assay. A low K-d value (1.046 mu M) suggested high binding of peptide with ochratoxin A. The potential of peptide-based ochratoxin A recognition was translated to a portable platform using streptavidin functionalized AuNPs conjugated to a biotinylated 11-mer peptide. Dot-blot assay was developed for detection of ochratoxin A with a limit of detection of 0.49 mu g/kg. Negligible cross-reactivity with low spot intensities were observed for high concentrations of other mycotoxins like aflatoxin B1 and citrinin, in comparison to control. Further, percent recovery of ochratoxin A from spiked wheat samples by dot-blot was comparable to the conventional high performance liquid chromatography (HPLC). Moreover, detection of ochratoxin A by dot-blot was validated by HPLC in 65 whole wheat, crushed wheat coarse, crushed wheat fine and wheat flour samples with a high correlation with R-2 = 0.93. HPLC and dot blot confirmed the presence of ochratoxin A < 5 mu g/kg in the samples. Therefore, a portable, easy-to-use dot-blot assay for ochratoxin A detection with potential of application at each stage of harvesting, storage, production and distribution can contribute to safe and healthy food and feed.
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